Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family

Komara Makanko; John Anne; Suleiman Jehan; Ali Bassam R.; Al-Gazali Lihadh

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Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family

机译：近交阿拉伯家庭中2型失衡综合症和严重的感音神经性听力丧失的临床和分子鉴定

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来源
《American journal of medical genetics, Part A》 |2016年第2期|共4页
作者
Komara Makanko; John Anne; Suleiman Jehan; Ali Bassam R.; Al-Gazali Lihadh;
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正文语种 eng
中图分类医学遗传学;
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1. Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family [J] . Komara Makanko, John Anne, Suleiman Jehan, American journal of medical genetics, Part A . 2016,第2期

机译：近交阿拉伯家庭中2型失衡综合症和严重的感音神经性听力丧失的临床和分子鉴定
2. Clinical and molecular genetic analysis of a family with macrothrombocytopenia and early onset sensorineural hearing loss. [J] . Mhatre AN, Janssens S, Nardi MA European journal of medical genetics . 2009,第4期

机译：患有大血小板减少症和早期发作的感音神经性听力减退的家庭的临床和分子遗传学分析。
3. Oral-Facial-Digital Syndrome Type 1: Further Clinical and Molecular Delineation in 2 New Families [J] . The Cleft palate-craniofacial journal: official publication of the American Cleft Palate-Craniofacial Association . 2020,第5期

机译：口腔面部数字综合征1：进一步临床和分子描绘在2家新家
4. Digital Hearing Aid for Sensorineural Hearing Loss : (Ski-Slope Hearing Loss) [C] . K Arpitha Nagesh, P Kavya, B K Kavyashree, 2017 International Conference on Current Trends in Computer, Electrical, Electronics and Communication . 2017

机译：用于感觉神经性听力损失的数字助听器：（滑雪坡听力损失）
5. Significance of Endolymphatic Hydrops in Ears With Unilateral Sensorineural Hearing Loss [D] . Okazaki Yuriko, 岡崎由利子 2019

机译：单侧感觉神经性听力损失的耳朵内淋巴积水的意义
6. Mutations in the Wolfram Syndrome Type 1 Gene (WFSI) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss [O] . Marci M. Lesperance, James W. Hall III, Theresa B. San Agustin, -1

机译：Wolfram综合征1型基因（WFSI）中的突变定义了主要的低频感觉神经性听力损失的临床实体
7. Mutations in the Wolfram Syndrome Type 1 Gene (WFS1) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss [O] . Marci M. Lesperance, James W. Hall, Theresa B. San Agustin, 2003

机译：Wolfram综合征1基因（WFS1）中的突变定义了主导低频感觉损失的临床实体

Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family

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